Artificial si joint

ABSTRACT

An artificial SI-Joint includes a sacrum component and an ilium component. The sacrum component may include a ridge, foundation, perimeter surface and a fitting member. The ilium component may include a polybearing, edge, foundation, perimeter surface, and a ridge or sockets. The fitting member of the sacrum component may engage the polybearing of the ilium component to restore normal movement of the SI-Joint. The artificial SI-Joint may be implanted as a single unit or as separate pieces that are coupled together.

CROSS REFERENCE TO RELATED APPLICATIONS

This patent application is a continuation of U.S. patent applicationSer. No. 13/791,837, titled “ARTIFICIAL SI JOINT,” filed Mar. 8, 2013,now U.S. Pat. No. 8,778,026, which claims priority to U.S. ProvisionalPatent Application No. 61/609,195, titled “ARTIFICIAL SI JOINT,” andfiled Mar. 9, 2012, each of which is herein incorporated by reference inits entirety.

INCORPORATION BY REFERENCE

All publications and patent applications mentioned in this specificationare herein incorporated by reference to the same extent as if eachindividual publication or patent application was specifically andindividually indicated to be incorporated by reference.

FIELD

The present invention generally relates to an artificial sacroiliacjoint prosthesis. In various respects, the invention is directed to asacroiliac joint prosthesis for movably connecting the sacrum to theilium.

BACKGROUND

The human hip girdle (see FIGS. 1 and 2) is made up of three large bonesjoined by two relatively immobile joints. One of the bones is called thesacrum and it lies at the bottom of the lumbar spine, where it connectswith the L5 vertebra. The other two bones are commonly called “hipbones” and are technically referred to as the right ilium and the leftilium. The sacrum connects with both hip bones at the left and rightsacroiliac joints (SI-Joint).

The SI-Joint is a diarthrodial joint and operates to transfer largemechanical loads between the low back and the legs, while simultaneouslyallowing enough movement for the spine and extremities to functionnormally during daily activities. The sacral side of the SI-Jointcontains hyaline cartilage that moves against fibrocartilage on theiliac side. The joint is generally L-shaped with ridges and depressionsthat interlock the sacrum and the ilium. This interlocking increasesfriction and minimizes motion allowing the joint to have a small amountof movement.

When the joint has excessive motion, normal function of SI-Joint can bedisrupted and the joint may become inflamed causing pain. The SI-Jointhas been described as a pain generator for up to 22% of lower back pain.To relieve pain generated from the SI-Joint and restore normal functionof the SI-Joint, surgical treatment may be indicated. For example,surgical treatment may be indicated for degenerative sacroiliitis,inflammatory sacroiliitis, iatrogenic instability of the sacroiliacjoint, osteitis condensans ilii, or traumatic fracture dislocation ofthe pelvis. Currently, problems associated with the SI-Joint aretypically treated non-surgically with medications, limiting activity,undergoing a therapy and exercise program, or radiofrequency ablation.For more serious SI-Joint problems, surgery may be performed to fuse theSi-joint, eliminating motion between the sacrum and the ilium.

There is a need for improved treatments for addressing chronic hip,joint or back pain caused by the SI-Joint.

SUMMARY OF THE DISCLOSURE

The present invention generally relates to an artificial sacroiliacjoint prosthesis. In various respects, the invention is directed to asacroiliac joint prosthesis for connecting the sacrum to the ilium andpreserving motion therebetween.

Some embodiments described herein provide for an artificial SI-Jointimplant for placement in a sacrum, the implant having a foundationhaving an outer edge, a first surface, and a second surface, the firstsurface opposite the second surface; a curved ridge attached to thefirst surface of the foundation, the curved ridge having a first end anda second end, the first and second ends located inward of the outeredge, wherein the curved ridge is configured to project from the firstsurface of the foundation; a fitting member attached to the secondsurface of the foundation, the fitting member having a concave shapeconfigured to interface with an ilium implant.

In some embodiments, the sacrum implant has a curved ridge that iscoupled to and extends from the foundation. In some embodiments, thecurved ridge includes a curved cross-section. In other variations, thecurved ridge includes a bell-shaped cross-section. In furtherembodiments, the curved ridge is configured for insertion into thesacrum.

In any of the preceding embodiments, the first surface of the foundationincludes a flat surface that seamlessly meets the curved ridge. Thefoundation may also include a perimeter surface having an upper edge andthe curved ridge is located inward of the upper edge. The perimetersurface may extend around a periphery of the foundation.

In any of the preceding embodiments, the ridge may have a first radiusof curvature adapted to match a second radius of curvature for a bearingsurface of the implant or another articulating implant.

In further embodiments, the implant may include a coating covering theridge and the foundation, wherein the coating is conducive to bonyin-growth. The coating may be a porous plasma spray coating. In someembodiments, the coating is formed from titanium or a titanium alloy. Inother embodiments, the coating comprises a biologic aid adapted topromote bony in-growth. The biologic aid may include a growth factor. Inother embodiments, the coating includes an antimicrobial agent.

In any of the preceding embodiments, the fitting member is adapted toengage a convex polybearing.

Additionally, in any of the preceding embodiments, the implant includesa proximal end, a distal end, and a length extending between theproximal and distal ends, the length being between about 20 mm to about100 mm.

In any of the preceding embodiments, the implant has a width betweenabout 1 cm to about 7 cm. In other embodiments, the implant has a heightbetween about 10 mm to about 40 mm.

Additional embodiments described herein provide for an artificialSI-Joint implant for placement in an ilium having a base having an outeredge; a ridge attached to a bone-interfacing surface of the base, theridge adapted for insertion into the ilium; and a polybearing located ona bearing surface of the base opposite the bone-interfacing surface, thebearing surface having an edge and the polybearing located inward of theedge, wherein the bearing surface is adapted to engage a sacrum implant.

In some embodiments, the polybearing has an oval shape. In otherembodiments, the polybearing is formed from a thermoplastic polymer. Infurther embodiments, the polybearing includes a convex surface curvingoutward from the base.

In any of the preceding embodiments, the base includes a perimetersurface, the perimeter surface having an oval circumference.

In further embodiments, the ridge includes a curved profile.Additionally, the ridge and base may be coated with a bony in-growthpromoting coating. In any of the preceding embodiments, the ridge mayhave a first radius of curvature adapted to match a second radius ofcurvature for a bearing surface of the implant.

In any of the preceding embodiments, the implant may have a proximalend, a distal end, and a length extending between the ends, the lengthbeing between about 20 mm to about 100 mm. In some embodiments, theimplant may have a width between about 1 cm to about 7 cm. In any of thepreceding embodiments, the implant may have a height between about 10 mmto about 40 mm.

In any of the preceding embodiments, the implant may include a mount onthe base, the mount having a notch for engaging a groove in thepolybearing to retain the polybearing.

Further embodiments described provide for an artificial SI-Jointincluding a sacrum component having a foundation with a first side and asecond side, the first side coupled to a sacrum ridge and the secondside coupled to a fitting member; and an ilium component having a baseincluding a third side and a fourth side opposite the third side, thethird side having a polybearing adapted for engaging the fitting memberof the sacrum component to allow movement of the ilium component orsacrum component relative to the other component.

In some embodiments, the sacrum component is configured to be coupled toa sacrum bone of a patient and the ilium component is configured to becoupled to the ilium bone of the patient.

In any of the preceding embodiments, the ilium component includes anilium ridge configured for insertion into the ilium, the ridge locatedon the fourth side of the ilium. In any of the preceding embodiments,the ilium ridge has a first radius of curvature adapted to match asecond radius of curvature for a bearing surface of the ilium component.In any of the preceding embodiments, the ilium component comprises asocket on the fourth side of the ilium, the socket adapted to receive ascrew through the ilium.

In any of the preceding embodiments, the sacrum ridge has a first radiusof curvature adapted to match a second radius of curvature for a bearingsurface of the sacrum component. In any of the preceding embodiments,the ridge of the sacrum component has a curved cross-section.

In any of the preceding embodiments, the polybearing is adapted to allowabout 2 degrees to about 4 degrees of movement. In any of the precedingembodiments, the fitting member is configured to engage and articulatewith the polybearing.

Other embodiments provide for methods of implanting an artificialSI-Joint implant. These methods include identifying an sacroiliacarticulation of a patient's SI-joint; creating a first insertion path inthe sacrum bone and a second insertion path the ilium bone of a patient;and inserting the implant into the first and second insertion paths inthe sacrum bone and ilium bone, wherein the implant comprises a sacrumcomponent for insertion into the sacrum bone and an ilium component forinsertion into the ilium bone.

In any of the preceding embodiments, the implant is inserted alongsacroiliac articulations.

In any of the preceding embodiments, the first and second insertionpaths are the same. In any of the preceding embodiments, the first andsecond insertion paths are curved. In further embodiments, the firstinsertion path includes a radius of curvature corresponding to a radiusof curvature for a ridge member on the sacrum component. In any of thepreceding embodiments, the radius of curvature for the first insertionpath is between about 10 mm to about 70 mm. In any of the precedingembodiments, the second insertion path includes a radius of curvaturecorresponding to a radius of curvature on a bearing surface of the iliumcomponent. In any of the preceding embodiments, the radius of curvaturefor the second insertion path is between about 10 mm to about 70 mm.

In any of the preceding embodiments, the methods include unlocking theimplant by removing a locking pin. In any of the preceding embodiments,the methods include rotating the implant during the inserting step.

In any of the preceding embodiments, the inserting step includesinserting a portion of the sacrum component and a portion of iliumcomponent into the sacrum and ilium respectively.

In any of the preceding embodiments, the methods include creating athird insertion path laterally through the ilium; and inserting a screwthrough the third insertion path to engage a socket of the artificialSI-Joint.

BRIEF DESCRIPTION OF THE DRAWINGS

The novel features of the invention are set forth with particularity inthe claims that follow. A better understanding of the features andadvantages of the present invention will be obtained by reference to thefollowing detailed description that sets forth illustrative embodiments,in which the principles of the invention are utilized, and theaccompanying drawings of which:

FIGS. 1-2 are, respectively, anterior and posterior views of the humanhip girdle.

FIG. 3 is an enlarged lateral view of the sacrum.

FIG. 4 is an enlarged lateral view of the sacral and lower lumbarregion.

FIG. 5 is a perspective view of the sacrum component of an exemplaryartificial SI-Joint.

FIG. 6 is a perspective view of the ilium component of an exemplaryartificial SI-Joint.

FIG. 7 is a cross-sectional view of an exemplary artificial SI-Joint.

FIG. 8 is a cranio-caudal section view of an implanted exemplaryartificial SI-Joint.

DETAILED DESCRIPTION

Reference will now be made in detail to exemplary embodiments of theinvention, examples of which are illustrated in the accompanyingdrawings. While the invention will be described in conjunction with theexemplary embodiments, it will be understood that they are not intendedto limit the invention to those embodiments. On the contrary, theinvention is intended to cover alternatives, modifications andequivalents, which may be included within the spirit and scope of theinvention as described herein.

Various aspects of the present invention relate to an artificialsacroiliac joint prosthesis. In various embodiments, the artificialjoint is implanted into the sacroiliac joint (SI-Joint).

FIGS. 1-2 are, respectively, anterior and posterior views of the humanhip girdle including the sacrum and the hip bones (the right ilium andthe left ilium), the sacrum being connected with both hip bones at theSI-Joints.

Each joint is encased and strengthened by two main ligaments, theinterosseous (not shown) and the posterior sacroiliac ligaments (notshown). The ligaments allow slight movement during non-weight bearingand less movement during weight bearing movements. The slight movementof the SI-Joint allows the joint to have enough play to provide spinalshock absorption, enhance lower extremity torque conversions andtransverse rotations.

The spine and the lower extremities are connected by the pelvis. Thespine movements occur in the sagittal plane and include flexion andextension. Hip movements may occur in all three planes, including arotational motion which the lumbar spine does not perform well. As aresult, the pelvic area should absorb the majority of lower extremityrotation, for example during bipedal gate.

FIG. 3 is an enlarged lateral view of the sacrum. FIG. 4 is an enlargedlateral view of the sacral and lower lumbar region. The sacrum 2includes an articular surface 4 that unites with the articular surfaceof the ilium (not shown). The sacroiliac articulations form the SI-Jointthat is a strong synovial joint between the sacrum and the ilium. TheSI-Joint contains numerous ridges and complimentary depressions thatprovide friction and help interlock the two bones. Additionally, thesacrum is wedged anteroposteriorly allowing it to provide resistance tovertical and horizontal translation as illustrated in FIGS. 1 and 2.Normal motion of the SI-Joint may include a combination of sliding,tilting and rotation. The SI-Joint may slide approximately 2 mm and maytilt or rotate approximately 2 to 4 degrees. The SI-Joint moves mostlyalong the sagittal plane about a point of rotation 6 and should not movein the transverse plane.

The artificial joint may be designed to replace the SI-Joint mimickingits shape and movement. The artificial joint may include a sacrumcomponent 11 and an ilium component 21. FIG. 5 is a perspective view ofthe sacrum component of an exemplary artificial SI-Joint. The sacrumcomponent 11 may include a ridge 12, a foundation 14, a perimetersurface 16, and a fitting member 18. The ridge 12 may be coupled to andextend away from the foundation 14. In some embodiments, the ridge 12has a generally uniform and curved cross section in the longitudinaldirection. In various embodiments, ridge 12 has a bell shape crosssection. Ridge 12 may include a proximal end 15 and a distal end 17. Theproximal end 15 and the distal end 17 of the ridge 12 may be flat andnot extend to the outer edge of foundation 14. Foundation 14 may includea generally flat surface that surrounds ridge 12. The outer edge offoundation 14 meets an upper edge 19 of perimeter surface 16. Ridge 12,foundation 14 and fitting member 18 may be formed from a polished metalor metal alloy including, but not limited to, cobalt chromium, titanium,tantalum, tivanium (aluminum, vanadium, and titanium), stainless steelor any other joint replacement metal.

Ridge 12 and foundation 14 may have a coating 20 that is conducive tobony in-growth, on-growth and/or through-growth. Coating 20 may beformed from titanium or titanium alloys. In some embodiments, thecoating 20 is a porous plasma spray coating. The coating 20 may create abiomechanically rigorous artificial joint prosthesis, designed tosupport acute weight bearing capacity. In various embodiments, the ridge12 and foundation 14 may be formed from a material that itselfinherently possesses a structure conducive to bony in-growth, on-growthand/or through-growth, such as a porous mesh, hydroxyapatite, or otherporous surface.

The coating 20 may include a material such as a biologic aid that maypromote and/or enhance bony in-growth, bony on-growth, bonythrough-growth, tissue repair, and/or reduce inflammation, infection andpain. The biologic aid may include growth factors, such as bonemorphogenetic proteins (BMPs), hydroxyapatite in a liquid or slurrycarrier, demineralized bone, morselized autograft or allograft bone,medications to reduce inflammation, infection and pain such asanalgesics, antibiotics and steroids. In various embodiments, the growthfactors may be human recombinant growth factors, such as rh-BMP-2 and/orrh-BMP-7, or any other human recombinant form of BMP. The carrier forthe biologic aid may be a liquid or gel such as saline or a collagengel.

The biologic aid may also be encapsulated or incorporated in acontrolled released formulation so that the biologic aid is released tothe patient at the implant site over a longer duration. For example, thecontrolled release formulation may be configured to release the biologicaid over the course of days, weeks or months, and can be configured torelease the biologic aid over an estimated time it would take for theimplant site to heal. The amount of biologic aid delivered to theartificial SI-Joint may be controlled using a variety of techniques,such as controlling or varying the amount of coating material applied tothe artificial SI-Joint and/or controlling or varying the amount ofbiologic aid incorporated into the coating material. Controlling theamount of biologic aid delivered may be important because excessive useof certain biologic aids may result in negative effects such aslocalized inflammation, local pain or radicular pain.

The coating 20 may further be covered with various other coatings suchas antimicrobial, antithrombotic, and osteoinductive agents, or acombination thereof. In various embodiments, the entire artificialSI-Joint may be impregnated with such agents.

Perimeter surface 16 extends around the periphery of foundation 14. Theperimeter surface 16 may be flat and form a shape that compliments thefitting member 18. In various embodiments, the perimeter surface 16forms a circumference that is bean-shaped. In some embodiments, theperimeter surface 16 has a coating 20. Perimeter surface 16 may beformed from similar materials as that described for ridge 12 andfoundation 14.

Fitting member 18 may have a concave surface and an outer edge (notshown). The concave surface may engage a convex polybearing 22 of theilium component 21 (see FIG. 6). The outer edge of the fitting member 18may engage an outer edge 24 of the polybearing 22.

The sacrum component 11 has a length L_(S) that extends from theproximal end 25 to the distal end 27 of sacrum component 11. In someembodiments, the length L_(S) may be within a range of about 20 mm to100 mm. The length L_(S) may be about 20 mm, 40 mm, 60 mm, 80 mm, or 100mm.

FIG. 6 is a perspective view of the ilium component of an exemplaryartificial SI-Joint. The ilium component 21 may include polybearing 22,edge 24, perimeter surface 26, foundation 28, ridge 30 and coating 32.Polybearing 22 may have a bean shape. Polybearing 22 may be formed fromone or more of a thermoplastic polyethylene (e.g. ultra-high molecularweight polyethylene, high-modulus polyethylene or high-performancepolyethylene), organic polymer thermoplastic (e.g. polyether etherketone), thermoset polymer, elastomer, pyrocarbon and other material. Inalternative embodiments, a polybearing may be located on the sacrumcomponent 11 (FIG. 5) while a metal or metal alloy bearing is located onthe ilium component 21 (FIG. 6). In some embodiments, both the sacrumcomponent 11 and the ilium component 21 may be made of metal or metalalloy, such as stainless steel.

The surface of polybearing 22 may be convex and may extend away fromedge 24. Edge 24 may extend around the perimeter of polybearing 22. Edge24 may have a rough or treated surface designed to increase frictionwhen engaging a surface of fitting member 18. Edge 24 and polybearing 22may engage a corresponding edge (not shown) and concave fitting member18, respectively, of the sacrum component 11.

Perimeter surface 26 may extend between the edge 24 and the rim offoundation 28. The perimeter surface 26 may be flat and form a shapethat is complimentary to the shape of polybearing 22. In variousembodiments, the perimeter surface 26 forms a circumference that is beanshaped. Perimeter surface 26 may be formed from similar materials asthose described with respect to perimeter surface 16 of the sacrumcomponent 11.

The ridge 30 may be coupled to and extend away from the foundation 28.In some embodiments, the ridge 30 has a generally uniform and curvedcross section in the longitudinal direction. In various embodiments,ridge 30 has a bell shape cross section. Ridge 30 may include a proximalend 15 and a distal end 17. The proximal end 15 and the distal end 17 ofthe ridge 30 may be flat and not extend to the outer edge of foundation28. Foundation 28 may include a generally flat surface that surroundsridge 30. The outer edge of foundation 28 meets an upper edge 31 ofperimeter surface 26. Ridge 30 and foundation 28 may be formed fromsimilar materials as those described with respect to ridge 12 andfoundation 14 of the sacrum component 11. Ridge 30 and foundation 28 mayhave a coating 32. In some embodiments, the coating 32 may be porous.Coating 32 may be formed from similar materials as those described forcoating 20 of the sacrum component 11.

The ilium component 21 has a length L_(I) that extends from the proximalend 25 to the distal end 27 of ilium component 21. In some embodiments,the length L_(I) may be within a range of about 20 mm to about 100 mm.The length L_(I) may be about 20 mm, 40 mm, 60 mm, 80 mm, or 100 mm.

FIG. 7 is a cross-sectional view of an exemplary artificial SI-Joint.The exemplary artificial SI-Joint 41 includes sacrum component 11 andilium component 21. The sacrum component 11 includes ridge 12, coating20, perimeter 16 and fitting member 18. Fitting member 18 has a concaveshape that engages the convex shape of polybearing 22. The sacrumcomponent 11 has a height H_(S) that extends from a first point 42 oncoating 20 at the top of ridge 12 to the lower edge 23 of perimeter 16.In some embodiments, the height H_(S) may be within a range of about 10mm to 40 mm. The height H_(s) may be about 10 mm, 15 mm, 20 mm, 25 mm,30 mm, 35 mm or 40 mm.

The sacrum component 11 has a width W_(S) that extends from a first edge38 of the perimeter surface 16 to a second edge 40 of perimeter surface16. In some embodiments, the width of W_(S) may be within a range ofabout 1 cm to 7 cm. The width W_(S) may be about 1 cm, 2 cm, 3 cm, 4 cm,5 cm, 6 cm or 7 cm.

The ilium component 21 includes ridge 30, coating 32, perimeter surface26, and polybearing 22. The ilium component 21 has a height H_(I) thatextends from a first point 44 on the coating 32 of ridge 30 to a secondpoint 46 on polybearing 22. In some embodiments, the height of H_(I) maybe within a range of about 10 mm to 40 mm. The height H_(I) may be about10 mm, 15 mm, 20 mm, 25 mm, 30 mm, 35 mm or 40 mm.

The ilum component 21 has a width W_(I) that extends from a first edge48 to a second edge 50 of the perimeter surface 26. In some embodiments,the width W_(I) may be within a range of about 1 cm to 7 cm. The widthW_(I) may be about 1 cm, 2 cm, 3 cm, 4 cm, 5 cm, 6 cm or 7 cm. Invarious embodiments, W_(S) is larger than W_(I) to allow for rotation ofthe artificial SI-Joint 41. For example, W_(S) may be 7 cm and W_(I) maybe 8 cm to allow for approximately 2 to 4 degrees of rotation.

The ilium component 21 may include a first portion and a second portion.The first portion may include ridge 30, foundation 28, perimeter surface26, and coating 32. The second portion may include polybearing 22. Thefirst portion may also include mount 53 that fits into a notch inpolybearing 22. The cross section shape of mount 53 may form a knob andmay extend in the longitudinal direction between the proximal end anddistal end. The mount 53 may be formed from similar materials asdescribed with respect to ridge 30, foundation 28, and perimeter surface26.

FIG. 8 is a cranio-caudal section view of an implanted exemplaryartificial SI-Joint. The artificial SI-Joint 61 includes a sacrumcomponent having ridge 12, foundation 14, perimeter surface 16, fittingmember 18, coating 20 and edge 23. The artificial SI-Joint 61 alsoincludes an ilium component having polybearing 22, foundation 28, andsockets 52. The polybearing 22 may engage fitting member 18 which allowsmovement about the sacrum 2 in the sagittal plane. The artificialSI-Joint may move in the range of about 2 to 4 degrees. Sockets 52 mayreceive screws 54 laterally through bone of the ilium 3. In the sacrumcomponent, ridge 12 may be formed as a first piece and foundation 14,perimeter surface 16, and fitting member 18 may be formed as a secondpiece. In the ilium component, foundation 28 and sockets 52 may form athird piece and polybearing 22 may form a fourth piece.

The artificial SI-Joint like that shown in FIGS. 5-8 may be used toreplace a damaged or dysfunctional SI-Joint. The artificial SI-Joint maybe effectively implanted through the use of alternative surgicalapproaches; namely, a posterior inferior approach or a posteriorsuperior approach. The surgical procedure is desirably aided byconventional lateral and/or anterior- posterior (A-P) visualizationtechniques, e.g., using X-ray image intensifiers such as a C-arms orfluoroscopes to produce a live image feed that is displayed on a TVscreen.

To implant the artificial SI-joint into a patient, a physician mayidentify the SI-joint and the sacroiliac articulations of the SI-Joint.The artificial SI-Joint may be inserted along the surface of thesacroiliac articulations. Before insertion, the physician may identifywhere to place the pilot insertion path or bore through each of thesacrum bone segment and ilium bone segment. A single drill bit, multipledrill bits, reamer or other device may be employed to bore into the bonesurfaces to create a pilot bore of the desired size and configuration.The physician may then insert the artificial SI-Joint into the boredportion of the sacrum 2 and ilium 3. In some embodiments, a curvedinsertion path or bore is formed in one or both of the sacrum and ilium,matching the radius of curvature of curved ridge(s) of the sacrumcomponent and/or the ilium component. The radius of curvature of theridges may be selected to match a radius of curvature of the bearingsurfaces of the sacrum component and ilium component. This will allowthe artificial joint to rotate about a point of rotation 6, as shown inFIG. 3. In some embodiments, the point of rotation 6 is located outsideand posterior of the body (not shown.) In some embodiments, the radiusof the insertion path, ridges and bearing surfaces is within the rangeof about 10 mm and about 70 mm. In some embodiments, it may be 100 mm.In other embodiments, the insertion path and ridges may be straight.

In some embodiments, the artificial SI-Joint may be inserted as a singleunit into the SI-Joint with a locking pin. The locking pin may beremoved from the artificial SI-Joint after the joint is in position. Insome embodiments, the artificial SI-Joint may be inserted in pieces intothe bore portions of the sacrum 2 and the ilium 3. For example, ridge 12may first be inserted into the sacrum 2 as a first piece and foundation14, perimeter surface 16, and fitting member 18 may then be insertedinto the sacrum 2 as a second piece coupled to the first piece.Foundation 28 and sockets 52 may be inserted into the ilium as a thirdpiece and polybearing 22 may be inserted into the ilium as a fourthpiece coupled to the third piece.

Whether inserted as a single piece or multiple pieces, the artificialSI-Joint is inserted in such a manner as to avoid excessive damage tosurrounding ligaments and other tissue to maximize the effectiveness ofthe artificial SI-Joint. When the insertion paths are curved aspreviously described, the artificial joint may be rotated into place asit is inserted along the path.

In an embodiment that utilizes screws 54 and sockets 52, an insertionpath or bore may be formed from a lateral approach through the ilium tothe sockets 52 of the artificial SI-Joint ilium component. The screwsmay be inserted through the ilium and received by the sockets 52 tosecure the ilum component to the ilum.

The artificial SI-Joint makes possible a replacement prostheticSI-Joint. The design and configuration of the artificial SI-Joint mimicthe normal function of an SI-Joint allowing slight movement ofapproximately 2 to 4 degrees. A surface coating, for example a porousplasma spray coating with irregular surface, promotes bony in-growth,on-growth and/or through growth to provide a biomechanically rigorousprosthetic joint designed specifically to replace a dysfunctionalSI-Joint and stabilize the heavily loaded lumbar spine. To minimizetrauma to the ligaments and tissue, the artificial SI-Joint may beimplanted as a single unit or as separate pieces that are coupledtogether.

Additional details pertinent to the present invention, includingmaterials and manufacturing techniques, may be employed as within thelevel of those with skill in the relevant art. The same may hold truewith respect to method-based aspects of the invention in terms ofadditional acts commonly or logically employed. Also, it is contemplatedthat any optional feature of the inventive variations described may beset forth and claimed independently, or in combination with any one ormore of the features described herein. Likewise, reference to a singularitem, includes the possibility that there are plural of the same itemspresent. More specifically, as used herein and in the appended claims,the singular forms “a,” “and,” “said,” and “the” include pluralreferents unless the context clearly dictates otherwise. It is furthernoted that the claims may be drafted to exclude any optional element. Assuch, this statement is intended to serve as antecedent basis for use ofsuch exclusive terminology as “solely,” “only” and the like inconnection with the recitation of claim elements, or use of a “negative”limitation. Unless defined otherwise herein, all technical andscientific terms used herein have the same meaning as commonlyunderstood by one of ordinary skill in the art to which this inventionbelongs. The breadth of the present invention is not to be limited bythe examples described herein, but only by the plain meaning of theclaim terms employed.

What is claimed is:
 1. An artificial SI-Joint system, the systemcomprising: a first component having a foundation comprising a firstside and a second side, a first ridge extending from the first side, thesecond side having a concave and elongate articulating surface with afirst length and a first curvature along the first length; and a secondcomponent having a base comprising a third side and a fourth sideopposite the third side, the third side having a convex and elongatearticulating surface adapted for engaging the concave articulatingsurface of the first component to allow movement of the second componentrelative to the first component, wherein the convex articulating surfacehas a second length and a second curvature along the second length,wherein the first curvature matches the second curvature.
 2. The systemof claim 1, wherein the first component is configured to be coupled to asacrum bone of a patient and the second component is configured to becoupled to an ilium bone of the patient.
 3. The system of claim 1,wherein the second component comprises a second ridge extending from thefourth side of the second component.
 4. The system of claim 1, whereinthe second component comprises a socket on the fourth side of the secondcomponent, the socket adapted to receive a screw.
 5. The system of claim1, wherein the convex articulating surface and the concave articulatingsurface are adapted to allow about 2 degrees to about 4 degrees ofmovement relative to each other when engaged.
 6. The system of claim 1,wherein the first curvature and the second curvature both have a radiusof curvature between about 10 mm to about 70 mm.
 7. The system of claim1, wherein the first side of the first component and the fourth side ofthe second component are rough, while the concave articulating surfaceand the convex articulating surface are smooth.
 8. The system of claim1, wherein the first side of the first component and the fourth side ofthe second component are coated with a biologic aid.
 9. An artificialSI-Joint system, the system comprising: a first component having afoundation comprising a first side and a second side, a first ridgeextending from the first side, the second side having a convex andelongate articulating surface with a first length and a first curvaturealong the first length; and a second component having a base comprisinga third side and a fourth side opposite the third side, the third sidehaving a concave and elongate articulating surface adapted for engagingthe convex articulating surface of the first component to allow movementof the second component relative to the first component, wherein theconcave articulating surface has a second length and a second curvaturealong the second length, wherein the first curvature matches the secondcurvature.
 10. The system of claim 9, wherein the first component isconfigured to be coupled to a sacrum bone of a patient and the secondcomponent is configured to be coupled to an ilium bone of the patient.11. The system of claim 9, wherein the second component comprises asecond ridge extending from the fourth side of the second component. 12.The system of claim 9, wherein the second component comprises a socketon the fourth side of the second component, the socket adapted toreceive a screw.
 13. The system of claim 9, wherein the convexarticulating surface and the concave articulating surface are adapted toallow about 2 degrees to about 4 degrees of movement relative to eachother when engaged.
 14. The system of claim 9, wherein the firstcurvature and the second curvature both have a radius of curvaturebetween about 10 mm to about 70 mm.
 15. The system of claim 9, whereinthe first side of the first component and the fourth side of the secondcomponent are rough, while the concave articulating surface and theconvex articulating surface are smooth.
 16. The system of claim 9,wherein the first side of the first component and the fourth side of thesecond component are coated with a biologic aid.
 17. A method ofcreating an artificial SI-Joint in a patient, the method comprising:creating a first curved insertion path in the sacrum and a second curvedinsertion path in the ilium along articular bone within the patient'sSI-Joint, wherein the first curved insertion path and the second curvedinsertion path have matching curvatures with a common axis of rotation;inserting a sacrum component into the first insertion path; andinserting an ilium component into the second insertion path.
 18. Themethod of claim 17, wherein the step of inserting the sacrum componentcomprises rotating the sacrum component into the first insertion pathabout the common axis of rotation, and wherein the step of inserting theilium component comprises rotating the ilium component into the secondinsertion path about the common axis of rotation.
 19. The method ofclaim 17, further comprising aligning a concave articulating surface ofthe sacrum component with a convex articulating surface of the iliumcomponent.
 20. The method of claim 17, further comprising aligning aconvex articulating surface of the sacrum component with a concavearticulating surface of the ilium component.